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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6876 - 6900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:4617	periapical granuloma Aliases: Apical granuloma	Ccl7	287561	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2772	irritant dermatitis Aliases: irritant contact dermatitis primary irritant dermatitis	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9790	toxocariasis Aliases: Infection by Toxascaris Toxocara infection visceral larva migrans	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma Aliases: cutaneous T cell lymphoma cutaneous T-cell lymphoma	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050634	alopecia universalis Aliases: ALOPECIA UNIVERSALIS CONGENITA	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1495	cystic echinococcosis Aliases: Echinococcus granulosus infection Echinococcus granulosus infection of lung Echinococcus granulosus infection of thyroid Liver echinococcus granulosus Thyroid echinococcus granulosus echinococcus granulosus echinococcus granulosus infectious disease echinococcus granulosus infectious disease of liver echinococcus granulosus infectious disease of thyroid lung echinococcus granulosus unilocular echinococcosis unilocular hydatid disease	Il4 Tlr4	287287 29260	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050824	sinoatrial node disease Aliases: SA node sinuatrial node	ANK2	287	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111700	ankyrin-B-related cardiac arrhythmia Aliases: ankyrin-B syndrome	ANK2	287	Homo sapiens (human)	Alliance of Genome Resources
DOID:13839	extrapyramidal and movement disease	Cyp2d5	286963	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14764	Larsen syndrome Aliases: dominant larsen syndrome	Flnb	286940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050680	Boomerang dysplasia	Flnb	286940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080096	myofibrillar myopathy 5 Aliases: filaminopathy	Flnb Flnc	286940 68794	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111190	distal myopathy 4 Aliases: MPD4 distal ABD-filaminopathy distal muscular dystrophy 4 distal myopathy with posterior leg and anterior hand involvement	Flnb Flnc	286940 68794	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080095	myofibrillar myopathy 4 Aliases: zaspopathy	Pdlim5 Pdlim7	286908 64353	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2030	anxiety disorder Aliases: anxiety anxiety state	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080547	metabolic dysfunction-associated steatohepatitis Aliases: MASH NASH non-alcoholic steatohepatitis nonalcoholic steatohepatitis	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:11446	sciatic neuropathy	cacna1da cacna1ha fgfr1a gfra1a gfra1b mc4r pdgfra slc17a8	286833 30705 386856 403310 560875 563467 79376 79377	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	dgat2 fgfr1a ins mc4r mttp	286833 30262 30705 406207 565316	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110500	autosomal recessive nonsyndromic deafness 42 Aliases: DFNB42 autosomal recessive deafness 42	ILDR1	286676	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112274	X-linked spermatogenic failure 3 Aliases: SPGFX3	CFAP47	286464	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110526	autosomal recessive nonsyndromic deafness 79 Aliases: DFNB79 autosomal recessive deafness 79	TPRN	286262	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111134	focal segmental glomerulosclerosis 9 Aliases: FSGS9	CRB2	286204	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111625	ventriculomegaly - cystic kidney disease Aliases: VMCKD congenital nephrosis-cerebral ventriculomegaly syndrome cystic kidney disease with ventriculomegaly ventriculomegaly with cystic kidney disease	CRB2	286204	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112353	spermatogenic failure 64 Aliases: SPGF64	FBXO43	286151	Homo sapiens (human)	Alliance of Genome Resources

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